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本文引用的文献

1
Drosophila HNF4 regulates lipid mobilization and beta-oxidation.果蝇肝细胞核因子4调节脂质动员和β-氧化。
Cell Metab. 2009 Mar;9(3):228-39. doi: 10.1016/j.cmet.2009.01.009.
2
Triacylglycerol metabolism in adipose tissue.脂肪组织中的三酰甘油代谢。
Future Lipidol. 2007 Apr;2(2):229-237. doi: 10.2217/17460875.2.2.229.
3
Cdk1/Cdc28-dependent activation of the major triacylglycerol lipase Tgl4 in yeast links lipolysis to cell-cycle progression.酵母中主要三酰甘油脂肪酶Tgl4的Cdk1/Cdc28依赖性激活将脂肪分解与细胞周期进程联系起来。
Mol Cell. 2009 Jan 16;33(1):53-63. doi: 10.1016/j.molcel.2008.12.019.
4
Advances in adipose tissue metabolism.脂肪组织代谢的进展。
Int J Obes (Lond). 2008 Dec;32 Suppl 7:S39-51. doi: 10.1038/ijo.2008.237.
5
AdPLA ablation increases lipolysis and prevents obesity induced by high-fat feeding or leptin deficiency.脂肪特异性磷脂酶A2缺失增加脂肪分解,并预防高脂喂养或瘦素缺乏诱导的肥胖。
Nat Med. 2009 Feb;15(2):159-68. doi: 10.1038/nm.1904. Epub 2009 Jan 11.
6
Adipose overexpression of desnutrin promotes fatty acid use and attenuates diet-induced obesity.去营养蛋白在脂肪组织中的过表达促进脂肪酸利用并减轻饮食诱导的肥胖。
Diabetes. 2009 Apr;58(4):855-66. doi: 10.2337/db08-1644. Epub 2009 Jan 9.
7
Adipose-specific knockout of raptor results in lean mice with enhanced mitochondrial respiration.雷帕霉素靶蛋白(Raptor)在脂肪组织中的特异性敲除导致小鼠变瘦,线粒体呼吸增强。
Cell Metab. 2008 Nov;8(5):399-410. doi: 10.1016/j.cmet.2008.09.003.
8
Insulin sensitivity: modulation by nutrients and inflammation.胰岛素敏感性:受营养物质和炎症的调节
J Clin Invest. 2008 Sep;118(9):2992-3002. doi: 10.1172/JCI34260.
9
Lipolysis and the integrated physiology of lipid energy metabolism.脂解作用与脂质能量代谢的整合生理学
Mol Genet Metab. 2008 Nov;95(3):117-26. doi: 10.1016/j.ymgme.2008.06.012. Epub 2008 Aug 31.
10
FSP27 contributes to efficient energy storage in murine white adipocytes by promoting the formation of unilocular lipid droplets.FSP27通过促进单房脂滴的形成,有助于小鼠白色脂肪细胞中高效的能量储存。
J Clin Invest. 2008 Aug;118(8):2808-21. doi: 10.1172/JCI34090.

脂肪的真相:脂肪细胞中的脂肪分解和脂肪酸利用。

The skinny on fat: lipolysis and fatty acid utilization in adipocytes.

机构信息

Department of Nutritional Science and Toxicology, University of California, Berkeley, California 9472, USA.

出版信息

Trends Endocrinol Metab. 2009 Nov;20(9):424-8. doi: 10.1016/j.tem.2009.06.002. Epub 2009 Sep 30.

DOI:10.1016/j.tem.2009.06.002
PMID:19796963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2764815/
Abstract

Lipolysis for the provision of fatty acids (FA) for other organs during times of energy demand occurs uniquely in white adipose tissue (WAT). Recent findings have identified a bona fide TAG hydrolase and the major adipose phospholipase A(2), AdPLA. By controlling PGE(2) levels, AdPLA dominantly regulates lipolysis in an autocrine/paracrine manner. Moreover, recent findings demonstrate that, surprisingly, increasing lipolysis in adipose tissue does not necessarily increase serum FA levels, which are usually correlated with insulin resistance. Rather, increasing lipolysis in adipose tissue causes a shift within adipocytes towards increased FA utilization and energy expenditure and thus protects against obesity. Here, we discuss the regulation of lipolysis and its effects on FA utilization within WAT and on insulin resistance.

摘要

在能量需求时,脂肪组织(WAT)特有的脂解作用将脂肪酸(FA)供给其他器官。最近的研究发现了一种真正的 TAG 水解酶和主要的脂肪组织磷酸酶 A2(AdPLA)。通过控制 PGE2 水平,AdPLA 以自分泌/旁分泌方式主导脂解作用。此外,最近的研究发现,令人惊讶的是,增加脂肪组织中的脂解作用不一定会增加血清 FA 水平,而血清 FA 水平通常与胰岛素抵抗相关。相反,增加脂肪组织中的脂解作用会导致脂肪细胞内 FA 利用和能量消耗增加,从而防止肥胖。在这里,我们讨论了脂肪组织中脂解作用的调节及其对 FA 利用和胰岛素抵抗的影响。